Structural and functional evolution of the P2Y sub(12)-like receptor group

• Published in: Purinergic signalling 2007-09, Vol.3 (4), p.255-268
• Main Authors: Schoeneberg, Torsten, Hermsdorf, Thomas, Engemaier, Eva, Engel, Kathrin, Liebscher, Ines, Thor, Doreen, Zierau, Klaas, Roempler, Holger, Schulz, Angela
• Format: Article
• Language: English
• ISSN: 1573-9538; 1573-9546
• DOI: 10.1007/s11302-007-9064-0

Metabotropic pyrimidine and purine nucleotide receptors (P2Y receptors) belong to the superfamily of G protein-coupled receptors (GPCR). They are distinguishable from adenosine receptors (P1) as they bind adenine and/or uracil nucleotide triphosphates or diphosphates depending on the subtype. Over the past decade, P2Y receptors have been cloned from a variety of tissues and species, and as many as eight functional subtypes have been characterized. Most recently, several members of the P2Y sub(12)-like receptor group, which includes the clopidogrel-sensitive ADP receptor P2Y sub(12), have been deorphanized. The P2Y sub(12)-like receptor group comprises several structurally related GPCR which, however, display heterogeneous agonist specificity including nucleotides, their derivatives, and lipids. Besides the established function of P2Y sub(12) in platelet activation, expression in macrophages, neuronal and glial cells as well as recent results from functional studies implicate that several members of this group may have specific functions in neurotransmission, inflammation, chemotaxis, and response to tissue injury. This review focuses specifically on the structure-function relation and shortly summarizes some aspects of the physiological relevance of P2Y sub(12)-like receptor members.